← Back to catalogue

General Purpose Reaction Buffer

FDA UDI

Class I (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
General Purpose Reaction Buffer FDA UDI
Generic Name
pH-adjusted buffer solution IVD FDA UDI
Model / Reference
NB136 FDA UDI

Identifiers

Primary DI / UDI-DI
05051700020374 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
pH-adjusted buffer solution IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: pH-adjusted buffer solution IVD

General Purpose Reaction Buffer by The Binding Site Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as pH-adjusted buffer solution IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f9b58232-d575-4a5d-8f07-94e77dd99ac6 34 fields · synced May 30, 2026